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FDA 510(k)

AutoContour (RADAC V6)

K-Number: K262452 · 2026-08-14

Decision Date2026-08-14
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AutoContour (RADAC V6) is the device name listed in this FDA 510(k) record. The listed applicant is Radformation, Inc.. It received FDA 510(k) clearance on 2026-08-14 under 510(k) number K262452. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AutoContour (RADAC V6)?

AutoContour (RADAC V6) is a medical device that received FDA 510(k) clearance on 2026-08-14. The listed applicant is Radformation, Inc.. The 510(k) number is K262452.

When did AutoContour (RADAC V6) receive FDA 510(k) clearance?

AutoContour (RADAC V6) received FDA 510(k) clearance on 2026-08-14, under 510(k) number K262452.

Who is the listed applicant for AutoContour (RADAC V6)?

The FDA 510(k) record lists Radformation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AutoContour (RADAC V6)?

The FDA product code for AutoContour (RADAC V6) is QKB.

Other records listing Radformation, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 16 devices →

Related Devices (Code: QKB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.